Q92777 (SYN2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 103.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Synapsin-2 Alternative name(s): Synapsin II | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) [Reference proteome] | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 582 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Neuronal phosphoprotein that coats synaptic vesicles, binds to the cytoskeleton, and is believed to function in the regulation of neurotransmitter release By similarity. |
| Subunit structure | Interacts with CAPON By similarity. |
| Subcellular location | |
| Tissue specificity | Central and peripheral nervous systems. |
| Domain | The A region binds phospholipids with a preference for negatively charged species By similarity. |
| Post-translational modification | Phosphorylation at Ser-10 dissociates synapsins from synaptic vesicles By similarity. |
| Sequence similarities | Belongs to the synapsin family. |
| Caution | There are several mRNAs and ESTs supporting this gene model. However, the genome sequence encoding the N-terminal part contains several sequence discrepancies. |
| Sequence caution | The sequence AC022234 differs from that shown. Reason: Frameshift at position 71. The sequence AC022234 differs from that shown. Reason: Several in-frame stop codons. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Cell junction Synapse |
| Coding sequence diversity | Alternative splicing Polymorphism |
| PTM | Phosphoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | metabolic process Inferred from electronic annotation. Source: GOC neurotransmitter secretionInferred from electronic annotation. Source: InterPro synaptic transmissionTraceable author statement Ref.1. Source: ProtInc |
| Cellular_component | cell junction Inferred from electronic annotation. Source: UniProtKB-KW synaptic vesicleInferred from electronic annotation. Source: InterPro |
| Molecular_function | ATP binding Inferred from electronic annotation. Source: InterPro catalytic activityInferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform IIa (identifier: Q92777-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform IIb (identifier: Q92777-2) The sequence of this isoform differs from the canonical sequence as follows: 458-480: GPGQPQGMQPPGKVLPPRRLPPG → CLQYILDCNGIAVGPKQVQAS 481-582: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 582 | 582 | Synapsin-2 | PRO_0000183021 | |||||
Regions | |||||||||
| Region | 1 – 29 | 29 | A | ||||||
| Region | 33 – 112 | 80 | B; linker | ||||||
| Region | 113 – 420 | 308 | C; actin-binding and synaptic-vesicle binding | ||||||
| Region | 421 – 457 | 37 | G; Pro-rich linker | ||||||
| Region | 458 – 533 | 76 | H; Pro/Ser-rich linker | ||||||
| Region | 534 – 582 | 49 | E | ||||||
| Compositional bias | 34 – 42 | 9 | Poly-Pro | ||||||
| Compositional bias | 486 – 496 | 11 | Poly-Ser | ||||||
| Compositional bias | 512 – 516 | 5 | Poly-Ser | ||||||
Amino acid modifications | |||||||||
| Modified residue | 10 | 1 | Phosphoserine; by PKA and CaMK1 By similarity | ||||||
| Modified residue | 421 | 1 | Phosphothreonine By similarity | ||||||
| Modified residue | 425 | 1 | Phosphoserine By similarity | ||||||
Natural variations | |||||||||
| Alternative sequence | 458 – 480 | 23 | GPGQP…RLPPG → CLQYILDCNGIAVGPKQVQA S in isoform IIb. | VSP_006320 | |||||
| Alternative sequence | 481 – 582 | 102 | Missing in isoform IIb. | VSP_006321 | |||||
| Natural variant | 506 | 1 | T → A. Corresponds to variant rs794999 [ dbSNP | Ensembl ]. | VAR_059825 | |||||
Experimental info | |||||||||
| Sequence conflict | 34 | 1 | A → P Ref.1 | ||||||
| Sequence conflict | 34 | 1 | A → P in AAC28368. Ref.2 | ||||||
| Sequence conflict | 34 | 1 | A → P in AAC33789. Ref.2 | ||||||
| Sequence conflict | 36 | 1 | T → P Ref.1 | ||||||
| Sequence conflict | 36 | 1 | T → P in AAC28368. Ref.2 | ||||||
| Sequence conflict | 36 | 1 | T → P in AAC33789. Ref.2 | ||||||
| Sequence conflict | 61 | 1 | T → K in AAC28368. Ref.2 | ||||||
| Sequence conflict | 61 | 1 | T → K in AAC33789. Ref.2 | ||||||
| Sequence conflict | 61 | 1 | T → R in AAC50718. Ref.1 | ||||||
| Sequence conflict | 64 | 1 | A → P Ref.1 | ||||||
| Sequence conflict | 64 | 1 | A → P in AAC28368. Ref.2 | ||||||
| Sequence conflict | 64 | 1 | A → P in AAC33789. Ref.2 | ||||||
| Sequence conflict | 70 | 1 | P → A in AAC50718. Ref.1 | ||||||
| Sequence conflict | 71 | 1 | P → Q Ref.1 | ||||||
| Sequence conflict | 71 | 1 | P → Q in AAC28368. Ref.2 | ||||||
| Sequence conflict | 71 | 1 | P → Q in AAC33789. Ref.2 | ||||||
| Sequence conflict | 74 | 1 | R → P Ref.1 | ||||||
| Sequence conflict | 74 | 1 | R → P in AAC28368. Ref.2 | ||||||
| Sequence conflict | 74 | 1 | R → P in AAC33789. Ref.2 | ||||||
| Sequence conflict | 82 | 1 | L → F Ref.1 | ||||||
| Sequence conflict | 82 | 1 | L → F in AAC28368. Ref.2 | ||||||
| Sequence conflict | 82 | 1 | L → F in AAC33789. Ref.2 | ||||||
| Sequence conflict | 104 – 105 | 2 | GA → AP Ref.1 | ||||||
| Sequence conflict | 104 – 105 | 2 | GA → AP in AAC28368. Ref.2 | ||||||
| Sequence conflict | 104 – 105 | 2 | GA → AP in AAC33789. Ref.2 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Cloning and sequencing analysis of a human synapsin IIb-encoding brain cDNA." Xie Y. Gene 173:289-290(1996) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM IIB). Tissue: Brain. |
| [2] | "Cloning of cDNAs encoding human synapsins IIa and IIb." Porton B., Kao H.-T., Greengard P. DNA Seq. 10:49-54(1999) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS IIA AND IIB). Tissue: Brain. |
| [3] | "The DNA sequence, annotation and analysis of human chromosome 3." Muzny D.M., Scherer S.E., Kaul R., Wang J., Yu J., Sudbrak R., Buhay C.J., Chen R., Cree A., Ding Y., Dugan-Rocha S., Gill R., Gunaratne P., Harris R.A., Hawes A.C., Hernandez J., Hodgson A.V., Hume J. Gibbs R.A.Nature 440:1194-1198(2006) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | U40215 mRNA. Translation: AAC50718.1. AF077671 mRNA. Translation: AAC28368.1. AF077737 mRNA. Translation: AAC33789.1. AC022234 Genomic DNA. No translation available. AC026166 Genomic DNA. No translation available. AC091492 Genomic DNA. No translation available. |
| IPI | IPI00023302. IPI00186299. |
| UniGene | Hs.445503. |
3D structure databases | |
| ProteinModelPortal | Q92777. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q92777. 1 interaction. |
| STRING | 9606.ENSP00000342993. |
PTM databases | |
| PhosphoSite | Q92777. |
Polymorphism databases | |
| DMDM | 223634710. |
2D gel databases | |
| UCD-2DPAGE | Q92777. |
Proteomic databases | |
| PaxDb | Q92777. |
| PRIDE | Q92777. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Organism-specific databases | |
| GeneCards | GC03P012020. |
| HGNC | HGNC:11495. SYN2. |
| MIM | 600755. gene. |
| neXtProt | NX_Q92777. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG284201. |
| HOVERGEN | HBG016354. |
| InParanoid | Q92777. |
Enzyme and pathway databases | |
| Reactome | REACT_13685. Neuronal System. |
Gene expression databases | |
| CleanEx | HS_SYN2. |
| Genevestigator | Q92777. |
Family and domain databases | |
| Gene3D | 3.30.1490.20. 1 hit. 3.30.470.20. 2 hits. 3.40.50.20. 1 hit. |
| InterPro | IPR013815. ATP_grasp_subdomain_1. IPR013816. ATP_grasp_subdomain_2. IPR016185. PreATP-grasp_dom. IPR001359. Synapsin. IPR020898. Synapsin_ATP-bd_dom. IPR019735. Synapsin_CS. IPR019736. Synapsin_P_site. IPR020897. Synapsin_pre-ATP-grasp_dom. [Graphical view] |
| Pfam | PF02078. Synapsin. 1 hit. PF02750. Synapsin_C. 1 hit. PF10581. Synapsin_N. 1 hit. [Graphical view] |
| PRINTS | PR01368. SYNAPSIN. |
| SUPFAM | SSF52440. PreATP-grasp-like. 1 hit. |
| PROSITE | PS00415. SYNAPSIN_1. 1 hit. PS00416. SYNAPSIN_2. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| SOURCE | Search... |
Entry information
| Entry name | SYN2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q92777 Secondary accession number(s): A8MY98 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 3 Human chromosome 3: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

Clusters with
